For inhaled epoprostenol - see TIP SHEET for ordering
Monitoring :
Patients’ response to inhaled epoprostenol will be assessed by changes in oxygenation and hemodynamics:
Vital signs including blood pressure, heart rate, and oxygen saturations every 15 minutes for one hour during initial treatment and after each dose change, then per ICU protocol.
Other objective tools to assess efficacy of inhaled epoprostenol, including but not limited to invasive hemodynamic monitoring (e.g., pulmonary artery pressure monitoring, echocardiography).
Patients’ tolerability to inhaled epoprostenol will be assessed by signs and symptoms suggesting toxicity or intolerance:
Severe thrombocytopenia and bleeding
Worsening hemodynamics
Worsening oxygenation
Weaning and Discontinuation:
Weaning:
If weaning is appropriate, decrease rate by half for 30 minutes. If patient tolerated the half-rate, the discontinue therapy.
Weaning should be reconsidered and attending physician contacted if a patient demonstrates a decrease in oxygenation within 30 minutes of weaning.
Discontinuation:
Provider and treatment team will collaborate to determine if there was a reasonable clinical response (e.g. increase in PaO2/FiO2 of at least 10% or greater, improvements in hemodynamic or oxygenation parameters in response to reduction in pulmonary artery pressures). If no response is noted after 2 hours, inhaled epoprostenol therapy should be discontinued.
The half-life of epoprostenol is 3-6 minutes, and effect should be seen within 15 minutes of drug initiation. If there is no clinical effect after 2 to 4 hours, the drug should be discontinued.
Warning: Medical emergency if infusion interrupted; infuse through dedicated line.
Epoprostenol infusion requires an in-line 0.22 micron filter. See Filter Recommendations for IV Medications
Pulmonary Artery Hypertension: IV Admixture Tip Sheet (Legacy 6/2025)
Epoprostenol may only be ordered via Order Set. See 900.3233 Medications: Orders
For inhaled epoprostenol - see TIP SHEET for ordering